Your newpany

You’ll be joining a leading, research‑driven biopharmaceutical organisation with a strong UK & Ireland presence and large global footprint. The business manages a robust portfolio of centrally approved medicines and continues to invest in regulatory capability to support post‑approval lifecycle management andmercial growth across the UK&I markets.

Your new role

This is a Regulatory Affairs Manager mat cover position on a 12‑month contract, with the possibility of extension. The role sits within the UK & Ireland Regulatory Affairs function, reporting into the Head of UK Regulatory Affairs within the affiliate team.
The position will focus on post‑approval regulatory activities for centrally authorised (CP) products, with close collaboration across UK & Ireland stakeholders. The role will primarily support products within RRMS and will involve managingplex regulatory deliverables.
Key responsibilities may include:

Post‑a...